|Fri, 13 Oct 2006 17:13:57 +0200
|Thunderbird 184.108.40.206 (Windows/20060909)
Appropriately documents and validates statistical programs. Appropriately documents and validates statistical programs.
Police the protocols within manufacturing.
Writing master cleaning validation plans.
Design and develop examples for demonstrations. Hands on experience in physiological and pharmacological assessments and expertise in surgical skills in small animals is mandatory . Liaise with physicians and attend meetings.
Interact directly with developers to test software, resolve bugs, and incorporate quality in the SAS product during the development and QA cycle. In this role you will be responsible for study design, protocol preparation, in-life study conduct and monitoring, data evaluation and interpretation and reporting. Work with Business Analysts, gather functional requirements, and ensure that supported data model conforms to these requirements as well as modeling standards.
Provides ad hoc programming support for clinical or cross-functional teams.
Report to the Regulatory Affairs Director. Ensure conformance of validation protocols by all departments especially manufacturing.
BSc , PhD qualified in Chemistry or Physics.
Write planned process deviations. Degree in Chemistry or related discipline.
net architecture for use in SAS products such as Enterprise Guide, SWOJV. Research and implement appropriate statistical and machine learning methods. Degree in Life Sciences. Research and implement appropriate statistical and machine learning methods. Degree in Life Sciences.
Writing batch records. Ensure conformance of validation protocols by all departments especially manufacturing. Experience in writing and executing validation documentation.
|[Prev in Thread]
|[Next in Thread]